Difference between revisions of "Part:BBa K1413024"
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− | This part is composed by bphR1 promoter, from Pseudomonas | + | This part is composed by bphR1 promoter <a href="https://parts.igem.org/Part:BBa_K1155001">(BBa_K1155001)</a>, from Pseudomonas pseudoalcaligenes KF707, which allows the transcription of the genes of biphenyl degradation, the RBS <a href="https://parts.igem.org/Part:BBa_B0034">(BBa_B0034)</a>, RFP gene <a href="https://parts.igem.org/Part:BBa_E1010">(BBa_E1010)</a> and terminator <a href="https://parts.igem.org/Part:BBa_B0015">(BBa_B0015)</a>. In our project, genes of degradation was replaced by RFP gene to detect the compound. |
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Revision as of 22:00, 1 November 2014
bphR1-RBS-RFP-Terminator
This part is composed by bphR1 promoter (BBa_K1155001), from Pseudomonas pseudoalcaligenes KF707, which allows the transcription of the genes of biphenyl degradation, the RBS (BBa_B0034), RFP gene (BBa_E1010) and terminator (BBa_B0015). In our project, genes of degradation was replaced by RFP gene to detect the compound.
Mechanism explanation: In absence of PCBs, bphR2 (BBa_K1413021) is bound to bphR1 promoter which activate the transcription of RFP but in very low expression. In presence of PCBs, when compound diffuses into the media, it binds to bphr2 protein which undergoes a conformational change that permits to activate more stronger bphR1 promoter and increase the transcription of RFP.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 156
Illegal BamHI site found at 239
Illegal XhoI site found at 46 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 883
Illegal AgeI site found at 995 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 139